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Variable Changes in Genome Size Associated with Different Polyploid Events in Plantago (Plantaginaceae)

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/anbo.1998.0730openalex-snapshot

Plant Genome Size Estimation by Flow Cytometry: Inter-laboratory Comparison*1

inferredcites →https://doi.org/10.1016/b978-012301463-4/50004-8openalex-snapshot

Genome Size Evolution in Plants

inferredcites →https://doi.org/10.1016/j.tplants.2009.09.001openalex-snapshot

The flowering world: a tale of duplications

inferredcites →https://doi.org/10.1016/j.tplants.2010.06.001openalex-snapshot

Palaeogenomics of plants: synteny-based modelling of extinct ancestors

inferredcites →https://doi.org/10.1038/nature09916openalex-snapshot

Ancestral polyploidy in seed plants and angiosperms

inferredcites →https://doi.org/10.1071/sb09040openalex-snapshot

DNA sequences from three genomes reveal multiple long-distance dispersals and non-monophyly of sections in Australasian Plantago (Plantaginaceae)

inferredcites →https://doi.org/10.1073/pnas.92.17.7719openalex-snapshot

Rapid genome change in synthetic polyploids of Brassica and its implications for polyploid evolution.

inferredcites →https://doi.org/10.1080/0028825x.1967.10428752openalex-snapshot

COntributions to a chromosome atlas of the New Zealand flora—10

inferredcites →https://doi.org/10.1080/0028825x.1971.10430222openalex-snapshot

Contributions to a Chromosome Atlas of the New Zealand Flora—15 Miscellaneous Families

inferredcites →https://doi.org/10.1080/0028825x.1988.10410121openalex-snapshot

Notes on New Zealand Plantago species

inferredcites →https://doi.org/10.1080/0028825x.1989.10410373openalex-snapshot

Contributions to a chromosome atlas of the New Zealand flora — 30 miscellaneous species

inferredcites →https://doi.org/10.1080/0028825x.1992.10412897openalex-snapshot

Chromosome numbers, karyotypes, and nuclear DNA variation in Pratia Gaudin (Lobeliaceae)

inferredcites →https://doi.org/10.1080/0028825x.2003.9512832openalex-snapshot

Variation in DNA C‐value and haploid genome size in New Zealand native grasses

inferredcites →https://doi.org/10.1080/0028825x.2010.515598openalex-snapshot

New chromosome counts in New Zealand species of Plantago (Plantaginaceae)

inferredcites →https://doi.org/10.1080/0028825x.2010.518318openalex-snapshot

Testing species limits of New Zealand Plantago (Plantaginaceae) using internal transcribed spacer (ITS) DNA sequences

inferredcites →https://doi.org/10.1080/0028825x.2012.671179openalex-snapshot

A taxonomic revision of native New Zealand Plantago (Plantaginaceae)

inferredcites →https://doi.org/10.1086/657657openalex-snapshot

Amplified Fragment Length Polymorphism Data Reveal a History of Auto- and Allopolyploidy in New Zealand Endemic Species of Plantago (Plantaginaceae): New Perspectives on a Taxonomically Challenging Group

inferredcites →https://doi.org/10.1093/aob/mcg005openalex-snapshot

First Nuclear DNA C-values for 28 Angiosperm Genera

inferredcites →https://doi.org/10.1093/aob/mcg105openalex-snapshot

Analysis of Nuclear DNA Content in Capsicum (Solanaceae) by Flow Cytometry and Feulgen Densitometry

inferredcites →https://doi.org/10.1093/aob/mci007openalex-snapshot

When does Intraspecific C-value Variation become Taxonomically Significant?

inferredcites →https://doi.org/10.1093/aob/mci019openalex-snapshot

The Origin, Evolution and Proposed Stabilization of the Terms 'Genome Size' and 'C-Value' to Describe Nuclear DNA Contents

inferredcites →https://doi.org/10.1093/aob/mci281openalex-snapshot

Nuclear DNA Variation, Chromosome Numbers and Polyploidy in the Endemic and Indigenous Grass Flora of New Zealand

inferredcites →https://doi.org/10.1093/aob/mcq011openalex-snapshot

Stomatal vs. genome size in angiosperms: the somatic tail wagging the genomic dog?

inferredcites →https://doi.org/10.1093/genetics/147.3.1381openalex-snapshot

Rapid Elimination of Low-Copy DNA Sequences in Polyploid Wheat: A Possible Mechanism for Differentiation of Homoeologous Chromosomes

inferredcites →https://doi.org/10.1098/rspb.1972.0042openalex-snapshot

Nuclear DNA content and minimum generation time in herbaceous plants

inferredcites →https://doi.org/10.1105/tpc.010082openalex-snapshot

Allopolyploidy-Induced Rapid Genome Evolution in the Wheat (Aegilops–Triticum) Group

inferredcites →https://doi.org/10.1105/tpc.13.8.1735openalex-snapshot

Allopolyploidy-Induced Rapid Genome Evolution in the Wheat (Aegilops-Triticum) Group

inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00349.xopenalex-snapshot

Genome downsizing in polyploid plants

inferredcites →https://doi.org/10.1111/j.1095-8339.2010.01054.xopenalex-snapshot

Genome size in Polystachya (Orchidaceae) and its relationships to epidermal characters

inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01433.xopenalex-snapshot

Hybridization and genome size evolution: timing and magnitude of nuclear DNA content increases in Helianthus homoploid hybrid species

inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02528.xopenalex-snapshot

Genome size is a strong predictor of cell size and stomatal density in angiosperms

inferredcites →https://doi.org/10.1126/science.220.4601.1049openalex-snapshot

Rapid Flow Cytometric Analysis of the Cell Cycle in Intact Plant Tissues

inferredcites →https://doi.org/10.1126/science.264.5157.421openalex-snapshot

Stomatal Size in Fossil Plants: Evidence for Polyploidy in Majority of Angiosperms

inferredcites →https://doi.org/10.1266/jjg.69.513openalex-snapshot

Nuclear DNA content of ten rice species as determined by flow cytometry.

inferredcites →https://doi.org/10.1508/cytologia.52.733openalex-snapshot

Nuclear DNA variation in relation to cytological features of some species in the genus Plantago L.

inferredcites →https://doi.org/10.3732/ajb.0800079openalex-snapshot

Polyploidy and angiosperm diversification

inferredcites →https://doi.org/10.3732/ajb.0800400openalex-snapshot

Molecular evidence of reticulate evolution in the subgenus Plantago (Plantaginaceae)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/phytotaxa.303.3.6zenodo-depositor-declared

A new polyploid species of Mecardonia (Gratioleae, Plantaginaceae) from South America

inferred← citeshttps://doi.org/10.1007/s10722-023-01811-5openalex-snapshot

The nuclear DNA content, ploidy, and chromosome numbers in some species of Nitraria and associations with pollen characteristics

inferred← citeshttps://doi.org/10.1016/j.forc.2020.100275openalex-snapshot

Non-destructive DNA analysis of single pollen grains

inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111527openalex-snapshot

Polyploidy leads to phenotypic differences between tetraploid Kaempferia galanga var. latifolia and pentaploid K. galanga var. galanga (Zingiberaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.05.013openalex-snapshot

The application of high-throughput sequencing for taxonomy: The case of Plantago subg. Plantago (Plantaginaceae)

inferred← citeshttps://doi.org/10.1071/bt19054openalex-snapshot

Leaf micromorphology of 19 Mentha taxa

inferred← citeshttps://doi.org/10.1080/0028825x.2014.898664openalex-snapshot

In situ hybridization with genomic and rDNA probes reveals complex origins for polyploid New Zealand species of Plantago (Plantaginaceae)

inferred← citeshttps://doi.org/10.1080/11263504.2015.1014006openalex-snapshot

Genome size and plastid trnK-matK markers give new insights into the evolutionary history of the genus Lavandula L.

inferred← citeshttps://doi.org/10.1093/aob/mcab102openalex-snapshot

The nature of intraspecific and interspecific genome size variation in taxonomically complex eyebrights

inferred← citeshttps://doi.org/10.1093/aob/mcac051openalex-snapshot

Polyploidy on islands – concerted evolution and gene loss amid chromosomal stasis

inferred← citeshttps://doi.org/10.1093/aobpla/plw082openalex-snapshot

An examination of nucleotypic effects in diploid and polyploid cotton

inferred← citeshttps://doi.org/10.1093/dnares/dsad013openalex-snapshot

Genome assembly of the pioneer speciesPlantago majorL. (Plantaginaceae) provides insight into its global distribution and adaptation to metal-contaminated soil

inferred← citeshttps://doi.org/10.1111/1755-0998.12705openalex-snapshot

Development of genome‐ and transcriptome‐derived microsatellites in related species of snapping shrimps with highly duplicated genomes

inferred← citeshttps://doi.org/10.1111/boj.12276openalex-snapshot

Is genome downsizing associated with diversification in polyploid lineages ofVeronica?

inferred← citeshttps://doi.org/10.1111/gcb.15249openalex-snapshot

The methylome is altered for plants in a high CO2 world: Insights into the response of a wild plant population to multigenerational exposure to elevated atmospheric [CO2]

inferred← citeshttps://doi.org/10.1111/jse.12310openalex-snapshot

Genome size variation and evolution in the grape family Vitaceae

inferred← citeshttps://doi.org/10.1186/1471-2229-13-173openalex-snapshot

Morphological, cytological and metabolic consequences of autopolyploidization in Hylocereus (Cactaceae) species

inferred← citeshttps://doi.org/10.1186/s12864-019-5859-yopenalex-snapshot

Small, but surprisingly repetitive genomes: transposon expansion and not polyploidy has driven a doubling in genome size in a metazoan species complex

inferred← citeshttps://doi.org/10.17520/biods.2020450openalex-snapshot

Relationship between functional traits and genome size variation of angiosperms with different life forms

inferred← citeshttps://doi.org/10.21203/rs.3.rs-11010200/v1openalex-snapshot

Genome size variation in Stemodia species (Gratioleae-Plantaginaceae) and its relationship with morphological and environmental variables

inferred← citeshttps://doi.org/10.31274/td-20240329-570openalex-snapshot

Parallelism and convergence during independent domestication of cotton species

inferred← citeshttps://doi.org/10.3390/genes11091097openalex-snapshot

Differential Gene Expression with an Emphasis on Floral Organ Size Differences in Natural and Synthetic Polyploids of Nicotiana tabacum (Solanaceae)

inferred← citeshttps://doi.org/10.3390/plants11202684openalex-snapshot

Cytogenetics and Consequences of Polyploidization on Different Biotic-Abiotic Stress Tolerance and the Potential Mechanisms Involved

inferred← citeshttps://doi.org/10.3390/plants13192691openalex-snapshot

Comparative Plastomics of Plantains (Plantago, Plantaginaceae) as a Tool for the Development of Species-Specific DNA Barcodes

inferred← citeshttps://doi.org/10.3897/compcytogen.v10i4.10362openalex-snapshot

Chromosome numbers and DNA content in some species of Mecardonia (Gratiolae, Plantaginaceae)

inferred← citeshttps://doi.org/10.5662/wjm.v4.i1.26openalex-snapshot

Molecular biomarkers for grass pollen immunotherapy

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